SMAD4 Overexpression in Patients with Sleep Apnoea May Be Associated with Cardiometabolic Comorbidities.
Carolina Cubillos-ZapataAna JaureguizarRaquel CasitasSara García-TovarBegoña Sánchez-SánchezEster ZamarrónEduardo López-CollazoFrancisco García-RíoCarolina CubillosPublished in: Journal of clinical medicine (2020)
Obstructive sleep apnoea (OSA) is associated with several diseases related to metabolic and cardiovascular risk. Although the mechanisms involved in the development of these disorders may vary, OSA patients frequently present an increase in transforming growth factor beta (TGFβ), the activity of which is higher still in patients with hypertension, diabetes or cardiovascular morbidity. Smad4 is a member of the small mother against decapentaplegic homologue (Smad) family of signal transducers and acts as a central mediator of TGFβ signalling pathways. In this study, we evaluate Smad4 protein and mRNA expression from 52 newly diagnosed OSA patients, with an apnoea-hypopnoea index (AHI) ≥30 and 26 healthy volunteers. These analyses reveal that OSA patients exhibit high levels of SMAD4 which correlates with variation in HIF1α, mTOR and circadian genes. Moreover, we associated high concentrations of Smad4 plasma protein with the presence of diabetes, dyslipidaemia and hypertension in these patients. Results suggest that increased levels of SMAD4, mediated by intermittent hypoxaemia and circadian rhythm deregulation, may be associated with cardiometabolic comorbidities in patients with sleep apnoea.
Keyphrases
- transforming growth factor
- newly diagnosed
- epithelial mesenchymal transition
- end stage renal disease
- positive airway pressure
- ejection fraction
- obstructive sleep apnea
- chronic kidney disease
- type diabetes
- cardiovascular disease
- cell proliferation
- gene expression
- metabolic syndrome
- high intensity
- transcription factor
- single cell
- weight loss
- endothelial cells
- heart rate
- binding protein
- drug induced
- patient reported
- genome wide identification